rs749672064

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs749672064(C;T)

Make rs749672064(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

128588887

Gene

SPTAN1

is a	snp
is	mentioned by
dbSNP	rs749672064
dbSNP (classic)	rs749672064
ClinGen	rs749672064
ebi	rs749672064
HLI	rs749672064
Exac	rs749672064
Gnomad	rs749672064
Varsome	rs749672064
LitVar	rs749672064
Map	rs749672064
PheGenI	rs749672064
Biobank	rs749672064
1000 genomes	rs749672064
hgdp	rs749672064
ensembl	rs749672064
geneview	rs749672064
scholar	rs749672064
google	rs749672064
pharmgkb	rs749672064
gwascentral	rs749672064
openSNP	rs749672064
23andMe	rs749672064
SNPshot	rs749672064
SNPdbe	rs749672064
MSV3d	rs749672064
GWAS Ctlg	rs749672064

Max Magnitude

0

ClinVar
Risk	rs749672064(T;T)
Alt	rs749672064(T;T)
Reference	Rs749672064(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SPTAN1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.131351166C>T
CLNSRC
CLNACC	RCV000189548.1,